| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5284866 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
A general, simple and straightforward strategy for the synthesis of a novel series of 4,4-disubstituted 2,3,4,7-tetrahydroazepines is described. This route involves a one-pot Wittig olefination/N-allylation process on a five-membered hemi-aminal followed by a final ring closing metathesis reaction.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Mario Barberis, Pablo GarcÃa-Losada, Sehila Pleite, Juan Ramón RodrÃguez, José Francisco Soriano, Javier Mendiola,